CY1110605T1 - PROCEDURE FOR PREPARATION OF PYRIMIDINE UNIONS - Google Patents
PROCEDURE FOR PREPARATION OF PYRIMIDINE UNIONSInfo
- Publication number
- CY1110605T1 CY1110605T1 CY20101100025T CY101100025T CY1110605T1 CY 1110605 T1 CY1110605 T1 CY 1110605T1 CY 20101100025 T CY20101100025 T CY 20101100025T CY 101100025 T CY101100025 T CY 101100025T CY 1110605 T1 CY1110605 T1 CY 1110605T1
- Authority
- CY
- Cyprus
- Prior art keywords
- compound
- formula
- preparation
- alkyl
- group
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D239/22—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/716—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Catalysts (AREA)
Abstract
Παρέχονται μία διαδικασία για την παρασκευή μίας ένωσης του Τύπου (I) και ενδιαμέσων χρήσιμων σ' αυτήν. Η διαδικασία περιλαμβάνει την αντίδραση μίας ένωσης του τύπου R1-CO-CH2-E με μία ένωση του τύπου R2-CHX1X2 υπό την παρουσία μίας ένωσης του τύπου R3R4N-C(=NH)NH2 και ενός καταλύτη, για να σχηματιστεί έτσι μία διυδροπυριμιδίνη· και την οξείδωση της διυδροπυριμιδίνης για να σχηματιστεί μία ένωση του Τύπου (1). To R1 είναι Η ή μία αλκυλ ομάδα· το R2 είναι Η, μία αλκυλ ή αρυλ ομάδα· τα R3 και R4 είναι, το καθένα ανεξάρτητα, Η, αλκυλ ή αρυλ, ή τα R3 και R4 ενώνονται για να σχηματιστεί, μαζί με το άζωτο στο οποίο είναι αυτά προσαρτημένα, για να σχηματιστεί ένας 5 έως 7μελής ετεροκυκλικός δακτύλιος· το Ε είναι Η, μία μη υποκατεστημένη αλκυλ ομάδα, μία αρυλ ομάδα ή μία ομάδα απόσυρσης ηλεκτρονίων· και τα Χ1 και Χ2 είναι το καθένα ανεξάρτητα ομάδες αναχώρησης, ή τα Χ1 και Χ2 αντιπροσωπεύουν μαζί =O.A process is provided for the preparation of a compound of Formula (I) and intermediates useful therein. The process comprises reacting a compound of formula R1-CO-CH2-E with a compound of formula R2-CHX1X2 in the presence of a compound of formula R3R4N-C (= NH) NH2 and a catalyst to form a dihydropyrimidine; and the oxidation of dihydropyrimidine to form a compound of Formula (1). R1 is H or an alkyl group; R2 is H, an alkyl or aryl group; R3 and R4 are each independently H, alkyl or aryl, or R3 and R4 are joined to form together with nitrogen to which they are attached to form a 5 to 7 membered heterocyclic ring; E is H, an unsubstituted alkyl group, an aryl group or an electron withdrawing group; and X1 and X2 are each independently leaving groups, or X1 and X2 represent together = O.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0229243A GB0229243D0 (en) | 2002-12-16 | 2002-12-16 | Compounds and process |
GB0303589A GB0303589D0 (en) | 2003-02-17 | 2003-02-17 | Compounds and process |
GB0318515A GB0318515D0 (en) | 2003-08-07 | 2003-08-07 | Compounds and process |
EP03780362A EP1578731B1 (en) | 2002-12-16 | 2003-12-09 | Process for the preparation of pyrimidine compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
CY1110605T1 true CY1110605T1 (en) | 2015-04-29 |
Family
ID=32600665
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20101100025T CY1110605T1 (en) | 2002-12-16 | 2010-01-11 | PROCEDURE FOR PREPARATION OF PYRIMIDINE UNIONS |
Country Status (23)
Country | Link |
---|---|
US (2) | US7524955B2 (en) |
EP (2) | EP2088142A3 (en) |
JP (2) | JP4579821B2 (en) |
KR (1) | KR101060215B1 (en) |
AR (1) | AR042355A1 (en) |
AT (1) | ATE448209T1 (en) |
AU (1) | AU2003288443B2 (en) |
BR (1) | BR0317313A (en) |
CA (1) | CA2509344C (en) |
CY (1) | CY1110605T1 (en) |
DE (1) | DE60330050D1 (en) |
DK (1) | DK1578731T3 (en) |
ES (1) | ES2335279T3 (en) |
HK (1) | HK1080477A1 (en) |
IL (1) | IL168884A (en) |
MX (1) | MXPA05006425A (en) |
MY (1) | MY138051A (en) |
NO (2) | NO330983B1 (en) |
NZ (1) | NZ540722A (en) |
PT (1) | PT1578731E (en) |
SI (1) | SI1578731T1 (en) |
TW (1) | TWI322145B (en) |
WO (1) | WO2004054986A2 (en) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0011120D0 (en) | 2000-05-09 | 2000-06-28 | Avecia Ltd | Process |
NL1015744C2 (en) * | 2000-07-19 | 2002-01-22 | Dsm Nv | Process for the preparation of 2- (6-substituted-1,3-dioxan-4-yl) acetic acid derivatives. |
AU2002318041B2 (en) | 2001-07-13 | 2008-01-03 | Astrazeneca Uk Limited | Preparation of aminopyrimidine compounds |
EP1323717A1 (en) | 2001-12-27 | 2003-07-02 | Dsm N.V. | Process for the preparation of 2-(6-Substituted-1,3-Dioxane-4-yL) acetic acid derivatives |
KR20030092446A (en) * | 2002-05-29 | 2003-12-06 | 주식회사 한국토종약초연구소 | Composition comprising an extract of Lophatherum gracile BRONGN. Inhibiting HCV activity |
EP1375493A1 (en) | 2002-06-17 | 2004-01-02 | Dsm N.V. | Process for the preparation of an dioxane acetic acid ester |
GB0218781D0 (en) | 2002-08-13 | 2002-09-18 | Astrazeneca Ab | Chemical process |
ATE448209T1 (en) | 2002-12-16 | 2009-11-15 | Astrazeneca Uk Ltd | METHOD FOR PRODUCING PYRIMIDINE COMPOUNDS |
GB0312896D0 (en) * | 2003-06-05 | 2003-07-09 | Astrazeneca Ab | Chemical process |
UY28501A1 (en) | 2003-09-10 | 2005-04-29 | Astrazeneca Uk Ltd | CHEMICAL COMPOUNDS |
GB0324791D0 (en) * | 2003-10-24 | 2003-11-26 | Astrazeneca Ab | Chemical process |
GB0428328D0 (en) * | 2004-12-24 | 2005-02-02 | Astrazeneca Uk Ltd | Chemical process |
GB0514078D0 (en) * | 2005-07-08 | 2005-08-17 | Astrazeneca Uk Ltd | Chemical process |
US8153791B2 (en) | 2005-12-21 | 2012-04-10 | Janssen Pharmaceutica N.V. | Substituted pyrimidinyl oxime kinase inhibitors |
WO2007109783A2 (en) * | 2006-03-23 | 2007-09-27 | Janssen Pharmaceutica, N.V. | Substituted pyrimidine kinase inhibitors |
TW200831469A (en) * | 2006-12-01 | 2008-08-01 | Astrazeneca Uk Ltd | Chemical process |
BR112012029627B1 (en) | 2010-05-21 | 2020-11-10 | Cooper Technologies Company | adapter and method for coupling together |
Family Cites Families (39)
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US3278001A (en) * | 1965-02-02 | 1966-10-11 | Charles C Andrews | Bearing assembly for auger conveyors |
US4698340A (en) | 1984-07-19 | 1987-10-06 | Fujisawa Pharmaceutical Co., Ltd. | Pyrimidine derivatives, processes for preparation thereof and composition containing the same |
US4689414A (en) * | 1986-02-24 | 1987-08-25 | E. R. Squibb & Sons, Inc. | 2-(substituted imino)-6-aryl-3,6-dihydro-4-substituted-1,5(2H)-pyrimidinecarboxylic acids and analogs |
JPH03501613A (en) | 1988-10-06 | 1991-04-11 | サンド・アクチエンゲゼルシヤフト | Pyrimidinyl-substituted hydroxy acids, lactones and esters and pharmaceutical compositions containing them |
FR2665159B1 (en) | 1990-07-24 | 1992-11-13 | Rhone Poulenc Sante | NEW PYRIDINE AND QUINOLEIN DERIVATIVES, THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
JP2648897B2 (en) * | 1991-07-01 | 1997-09-03 | 塩野義製薬株式会社 | Pyrimidine derivatives |
WO1993008823A1 (en) | 1991-11-06 | 1993-05-13 | Tanabe Seiyaku Co., Ltd. | Guanidinyl and related cell adhesion modulation compounds |
JP3197971B2 (en) | 1993-03-01 | 2001-08-13 | 塩野義製薬株式会社 | Method for synthesizing 5-carboalkoxypyrimidine derivative |
US5593992A (en) * | 1993-07-16 | 1997-01-14 | Smithkline Beecham Corporation | Compounds |
NZ264063A (en) | 1993-08-13 | 1995-11-27 | Nihon Nohyaku Co Ltd | N-(2-phenylpyrid-3-yl)- and n-(4-phenylpyrimidin-5-yl)-n'-phenylurea derivatives and pharmaceutical compositions |
NZ297278A (en) | 1994-11-16 | 1999-06-29 | Synaptic Pharma Corp | 4-aryl dihydropyrimidine derivatives end medicaments |
DE19517186A1 (en) | 1995-05-11 | 1996-11-14 | Bayer Ag | Process for the preparation of substituted 2-fluoropyrimidines |
FR2741620B1 (en) | 1995-11-28 | 1997-12-26 | Oreal | PROCESS FOR THE PREPARATION OF COMPOUNDS WITH A BETA-HYDROXY -DELTA-LACTONE GROUP ANALOGS OF (+) COMPACTIN AND (+) MEVINOLINE |
US6278001B1 (en) | 1995-11-28 | 2001-08-21 | L'oréal | Method for preparing (+) compactin and (+) mevinolin analog compounds having a β-hydroxy-δ-lactone grouping |
SK77398A3 (en) | 1995-12-14 | 1999-02-11 | Merck & Co Inc | Process for making dihydropyrimidinones |
US5958934A (en) | 1996-05-23 | 1999-09-28 | Syntex (U.S.A.) Inc. | Aryl pyrimidine derivatives and uses thereof |
SE9702563D0 (en) | 1997-07-02 | 1997-07-02 | Astra Ab | Compounds |
CA2297889A1 (en) | 1997-08-05 | 1999-02-18 | Norihiro Ikemoto | Alpha 1a adrenergic receptor antagonist |
GB9903472D0 (en) | 1999-02-17 | 1999-04-07 | Zeneca Ltd | Chemical process |
AU5568400A (en) * | 1999-06-23 | 2001-01-09 | Ajinomoto Co., Inc. | Novel dihydropyrimidine derivatives |
HU228303B1 (en) * | 1999-07-13 | 2013-03-28 | Lonza Ag | Process for preparing 2-amino-4-(4-fluorphenyl)-6-alkylpyrimidine-5-carboxylate |
GB0003305D0 (en) | 2000-02-15 | 2000-04-05 | Zeneca Ltd | Pyrimidine derivatives |
WO2001072706A1 (en) | 2000-03-28 | 2001-10-04 | Biocon India Limited | Synthesis of [r-(r*,r*)]-2-(4-fluorophenyl)-beta,delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1h-pyrrole-1-heptanoic acid hemi calcium salt (atorvastatin) |
GB0011120D0 (en) | 2000-05-09 | 2000-06-28 | Avecia Ltd | Process |
GB0011163D0 (en) | 2000-05-10 | 2000-06-28 | Astrazeneca Ab | Chemical compound |
NL1015744C2 (en) | 2000-07-19 | 2002-01-22 | Dsm Nv | Process for the preparation of 2- (6-substituted-1,3-dioxan-4-yl) acetic acid derivatives. |
AU2002318041B2 (en) * | 2001-07-13 | 2008-01-03 | Astrazeneca Uk Limited | Preparation of aminopyrimidine compounds |
EP1323717A1 (en) | 2001-12-27 | 2003-07-02 | Dsm N.V. | Process for the preparation of 2-(6-Substituted-1,3-Dioxane-4-yL) acetic acid derivatives |
KR100511533B1 (en) | 2002-04-09 | 2005-08-31 | 임광민 | CHIRAL INTERMEDIATE, PROCESS FOR THE PRODUCTION THEREOF, AND PROCESS FOR THE PRODUCTION OF HMG-CoA REDUCTASE INHIBITOR |
EP1375493A1 (en) | 2002-06-17 | 2004-01-02 | Dsm N.V. | Process for the preparation of an dioxane acetic acid ester |
GB0218781D0 (en) | 2002-08-13 | 2002-09-18 | Astrazeneca Ab | Chemical process |
ATE448209T1 (en) | 2002-12-16 | 2009-11-15 | Astrazeneca Uk Ltd | METHOD FOR PRODUCING PYRIMIDINE COMPOUNDS |
WO2004103977A2 (en) | 2003-05-21 | 2004-12-02 | Ciba Specialty Chemicals Holding Inc. | Process for the preparation of pyrimidine derivatives |
GB0312896D0 (en) | 2003-06-05 | 2003-07-09 | Astrazeneca Ab | Chemical process |
UY28501A1 (en) | 2003-09-10 | 2005-04-29 | Astrazeneca Uk Ltd | CHEMICAL COMPOUNDS |
GB0321827D0 (en) | 2003-09-18 | 2003-10-15 | Astrazeneca Uk Ltd | Chemical compounds |
GB0324791D0 (en) | 2003-10-24 | 2003-11-26 | Astrazeneca Ab | Chemical process |
US20050159615A1 (en) | 2003-12-24 | 2005-07-21 | Entire Interest. | Process for preparation of statins with high syn to anti ratio |
GB0428328D0 (en) | 2004-12-24 | 2005-02-02 | Astrazeneca Uk Ltd | Chemical process |
-
2003
- 2003-12-09 AT AT03780362T patent/ATE448209T1/en active
- 2003-12-09 WO PCT/GB2003/005359 patent/WO2004054986A2/en active Application Filing
- 2003-12-09 MX MXPA05006425A patent/MXPA05006425A/en active IP Right Grant
- 2003-12-09 DK DK03780362.4T patent/DK1578731T3/en active
- 2003-12-09 SI SI200331722T patent/SI1578731T1/en unknown
- 2003-12-09 DE DE60330050T patent/DE60330050D1/en not_active Expired - Lifetime
- 2003-12-09 PT PT03780362T patent/PT1578731E/en unknown
- 2003-12-09 EP EP09159247A patent/EP2088142A3/en not_active Ceased
- 2003-12-09 US US10/537,723 patent/US7524955B2/en not_active Expired - Fee Related
- 2003-12-09 CA CA2509344A patent/CA2509344C/en not_active Expired - Fee Related
- 2003-12-09 JP JP2005502458A patent/JP4579821B2/en not_active Expired - Fee Related
- 2003-12-09 EP EP03780362A patent/EP1578731B1/en not_active Expired - Lifetime
- 2003-12-09 KR KR1020057010964A patent/KR101060215B1/en not_active IP Right Cessation
- 2003-12-09 AU AU2003288443A patent/AU2003288443B2/en not_active Ceased
- 2003-12-09 BR BR0317313-5A patent/BR0317313A/en not_active IP Right Cessation
- 2003-12-09 ES ES03780362T patent/ES2335279T3/en not_active Expired - Lifetime
- 2003-12-09 NZ NZ540722A patent/NZ540722A/en not_active IP Right Cessation
- 2003-12-10 AR ARP030104541A patent/AR042355A1/en unknown
- 2003-12-12 MY MYPI20034768A patent/MY138051A/en unknown
- 2003-12-16 TW TW092135557A patent/TWI322145B/en not_active IP Right Cessation
-
2005
- 2005-05-30 IL IL168884A patent/IL168884A/en not_active IP Right Cessation
- 2005-06-08 NO NO20052781A patent/NO330983B1/en not_active IP Right Cessation
-
2006
- 2006-01-12 HK HK06100506.1A patent/HK1080477A1/en not_active IP Right Cessation
-
2009
- 2009-03-16 US US12/404,575 patent/US8273878B2/en not_active Expired - Fee Related
-
2010
- 2010-01-11 CY CY20101100025T patent/CY1110605T1/en unknown
- 2010-06-23 JP JP2010142779A patent/JP5318037B2/en not_active Expired - Fee Related
-
2011
- 2011-03-10 NO NO20110366A patent/NO20110366L/en not_active Application Discontinuation
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